ACT in practice : case conceptualization in acceptance and commitment therapy
https://libcat.nshealth.ca/en/permalink/provcat24832
Bach, Patricia A.
--Oakland, CA:
New Harbinger Publications
, 2008.
- Call Number
- RC 489.C62 B118a 2008
- Location
- Nova Scotia Hospital
- Call Number
- RC 489.C62 B118a 2008
- Author
- Bach, Patricia A.
- Other Authors
- Moran, Daniel
- Place of Publication
- Oakland, CA
- Publisher
- New Harbinger Publications
- Date of Publication
- 2008
- Physical Description
- 334 p.
- ISBN
- 9781572244788
- Subjects (MeSH)
- Acceptance and Commitment Therapy
- Cognitive Behavioral Therapy - methods
- Adaptation, Psychological
- Mental Disorders - therapy
- Patient Participation
- Self Concept
- Contents
- An orientation to ACT -- Clinical behavior analysis and the three waves of behavior therapy -- Functional analysis and act assessment -- Relational frame theory -- What is case conceptualization? -- Conceptualizing functionally -- Contacting the present moment and perspective taking -- Values, commitment, and behavior change processes -- Acceptance processes -- Creative hopelessness : when the solution is the problem -- Bringing mindfulness to clinical work -- Values work -- Defusion and deliteralization -- Willingness -- Acceptance and change -- Pulling it all together.
- Format
- Book
- Location
- Nova Scotia Hospital
- Loan Period
- 3 weeks
Clinical Research Involving Pregnant Women
https://libcat.nshealth.ca/en/permalink/provcat41062
Françoise Baylis, Angela Ballantyne, editors.
--Cham:
Springer
, c2016.
- Available Online
- View e-Book
- Location
- Online
This book discusses "how" to respectfully and responsibly include pregnant women in clinical research. In sharp contrast, the existing literature predominantly focuses on the reasons "why" the inclusion of pregnant women in clinical research is necessary: viz., to develop effective treatments for women during pregnancy, to promote fetal safety, to reduce harm to women and fetuses from suboptimal care, and to allow access to the benefits of research participation. This book supports the shift to…
- Available Online
- View e-Book
- Other Authors
- Baylis, Françoise, 1961-
- Ballantyne, Angela
- Responsibility
- Françoise Baylis, Angela Ballantyne, editors
- Place of Publication
- Cham
- Publisher
- Springer
- Date of Publication
- c2016
- Physical Description
- 1 online resource (xv, 301 p.) : 1 illus.
- Series Vol.
- v. 3
- Series Title
- Research ethics forum
- ISBN
- 9783319265124
- 9783319265100 (print ed.)
- ISSN
- 2212-9529
- Subjects (MeSH)
- Clinical Trials as Topic - ethics
- Ethics, Research
- Patient Participation
- Pregnant Women
- Research Design
- Research Subjects
- Abstract
- This book discusses "how" to respectfully and responsibly include pregnant women in clinical research. In sharp contrast, the existing literature predominantly focuses on the reasons "why" the inclusion of pregnant women in clinical research is necessary: viz., to develop effective treatments for women during pregnancy, to promote fetal safety, to reduce harm to women and fetuses from suboptimal care, and to allow access to the benefits of research participation. This book supports the shift to a new default position, whereby pregnant women are included in clinical research unless researchers argue convincingly for their exclusion. This shift raises many as yet unexplored ethical and policy questions about existing barriers to the equitable inclusion of pregnant women in research. This book is original in three key ways. First, it presents an unparalleled depth of analysis of the ethics of research with pregnant women, bringing together many of the key authors in this field as well as experts in research ethics and in vulnerability who have not previously applied their work to pregnant women. Second, it includes innovative theoretical work in ethics and disease specific case studies that highlight the current complexity and future challenges of research involving pregnant women. Third, the book brings together authors who argue both for and against including more pregnant women in formal clinical trials.
- Contents
- 1. Missed Trials, Future Opportunities -- Part I -- 2. Why Physicians and Women Should Want Pregnant Women Included in Clinical Trials -- 3. Better Safe Than Sorry: Risk, Stigma, and Research During Pregnancy -- 4. Presumptive Inclusion and Legitimate Exclusion Criteria -- Part II -- 5. Fair Inclusion of Pregnant Women in Clinical Research: A Systematic Review of Reported Reasons for Exclusion -- 6. Research Ethics Review of Drug Trials Targeting Medical Conditions of Pregnant Women -- 7. Pregnant Women’s Views About Participation in Clinical Research -- Part III -- 8. Pregnancy, Vulnerability, and the Risk of Exploitation in Clinical Research -- 9. When Hypothetical Vulnerability Becomes Actual: Research Participation and the Autonomy of Pregnant Women -- 10. Equipoise, Uncertainty, and Inductive Risk in Research Involving Pregnant Women -- 11. Does My Bias Look Big in This? -- Part IV. 12. Research into Lifestyle Changes in Pregnancy -- 13. Ethics and Research with Pregnant Women: Lessons from HIV/AIDS -- 14. Ethical Issues in a Trial of Maternal Gene Transfer to Improve Foetal Growth -- 15. Clinical Research Involving Pregnant Women Seeking Abortion Services: United States Perspectives -- 16. Research on Uterine Transplantation: Ethical Considerations.
- Format
- e-Book
- Location
- Online
Consumer Health Informatics : Informing Consumers and Improving Health Care
https://libcat.nshealth.ca/en/permalink/provcat29632
edited by Deborah Lewis, Gunther Eysenbach, Rita Kukafka, P. Zoë Stavri, Holly B. Jimison.
--New York, NY:
Springer Science+Business Media
, c2005.
- Available Online
- View e-Book
- Location
- Online
- Available Online
- View e-Book
- Author
- Lewis, Deborah
- Other Authors
- Eysenbach, Gunther
- Kukafka, Rita
- Stavri, P. Zoë
- Jimison, Holly B
- Responsibility
- edited by Deborah Lewis, Gunther Eysenbach, Rita Kukafka, P. Zoë Stavri, Holly B. Jimison
- Place of Publication
- New York, NY
- Publisher
- Springer Science+Business Media
- Date of Publication
- c2005
- Series Title
- Health informatics
- ISBN
- 9780387276526
- Subjects (MeSH)
- Internet
- Medical Informatics
- Patient Participation
- Public Health Informatics
- Subjects (LCSH)
- Medical records - Data processing
- Public health
- Format
- e-Book
- Location
- Online
Consumers as providers in psychiatric rehabilitation
https://libcat.nshealth.ca/en/permalink/provcat20602
Mowbray, Carol T.
--Columbia, MD:
International Association of Psychosocial Rehabilitation Services
, 1997.
- Call Number
- WM 308 C766c 1997
- Location
- Nova Scotia Hospital
- Call Number
- WM 308 C766c 1997
- Author
- Mowbray, Carol T
- Place of Publication
- Columbia, MD
- Publisher
- International Association of Psychosocial Rehabilitation Services
- Date of Publication
- 1997
- Physical Description
- 525 p.
- ISBN
- 0965584313
- Subjects (MeSH)
- Mental Disorders - rehabilitation
- Mental Health Services
- Self-Help Groups
- Patient Participation
- Format
- Book
- Location
- Nova Scotia Hospital
- Loan Period
- 3 weeks
Critical decisions : how you and your doctor can make the right medical choices together
https://libcat.nshealth.ca/en/permalink/provcat25725
Peter A. Ubel.
--New York:
HarperOne
, c2012.
- Call Number
- WB 102 U13c 2012
- Location
- Dickson Building
- Halifax Infirmary
We've all been there, sitting uncomfortably in a paper gown as a doctor impassively describes our prognosis. Sometimes it's simple and treatable. Other times we get news we can't fathom and then are faced with decisions that are literally life and death. In this revolutionary book, physician, behavioral scientist, and bioethicist Peter Ubel, M.D., reveals how hidden dynamics in the doctor/patient relationship keep us and our loved ones from making the best medical choices. From doctors who str…
- Call Number
- WB 102 U13c 2012
- Author
- Ubel, Peter A
- Responsibility
- Peter A. Ubel
- Place of Publication
- New York
- Publisher
- HarperOne
- Date of Publication
- c2012
- Physical Description
- 360 p.
- ISBN
- 9780062103826
- 9780062103826 (hbk)
- Subjects (MeSH)
- Decision Making
- Physician-Patient Relations
- Patient Participation
- Abstract
- We've all been there, sitting uncomfortably in a paper gown as a doctor impassively describes our prognosis. Sometimes it's simple and treatable. Other times we get news we can't fathom and then are faced with decisions that are literally life and death. In this revolutionary book, physician, behavioral scientist, and bioethicist Peter Ubel, M.D., reveals how hidden dynamics in the doctor/patient relationship keep us and our loved ones from making the best medical choices. From doctors who struggle to explain, to patients who fail to properly listen, countless factors alter the course of our care, causing things to go seriously awry. With riveting stories of Ubel's own experience in the field, his groundbreaking research, and his personal journey walking loved ones through difficult treatment choices, Critical Decisions will forever change the way we communicate inside hospitals and medical offices, where thoughtful decision making matters the most.
- Contents
- Prologue: Who's in charge? -- Part I. The rise of the empowered patient -- Part II. Empowerment failure -- Part III. From empowerment to partnership -- Part IV. Learning to share.
- Format
- Book
- Location
- Dickson Building
- Halifax Infirmary
- Copies
- 2
- Loan Period
- 3 weeks
Enhancing Patient Engagement in Pulmonary Healthcare : The Art and Science
https://libcat.nshealth.ca/en/permalink/provcat45199
Marilyn L. Moy, Felicity Blackstock, Linda Nici, editors.
--Cham:
Humana Press
, c2020.
- Available Online
- View e-Book
- Location
- Online
This book examines the most up-to-date strategies that can be used to enhance the healthcare professional-patient interaction to influence positive behavior change and improve treatment adherence in pulmonary healthcare. This book is written by experts in the field who couple their experience with practical strategies (the art) with evidence-based theory (the science). Chapters discuss global concepts such as motivational interviewing on improving engagement and how to apply strategies to speci…
- Available Online
- View e-Book
- Other Authors
- Moy, Marilyn L.
- Blackstock, Felicity
- Nici, Linda
- Other Authors
- American Thoracic Society
- Responsibility
- Marilyn L. Moy, Felicity Blackstock, Linda Nici, editors
- Place of Publication
- Cham
- Publisher
- Humana Press
- Date of Publication
- c2020
- Physical Description
- 1 online resource (xi, 293 p.) : 60 illus., 47 illus. in color
- Series Title
- Respiratory medicine
- ISBN
- 9783030448899
- 9783030448882 (Print ed.)
- 9783030448905 (Print ed.)
- 9783030448912 (Print ed.)
- ISSN
- 2197-7372
- Subjects (MeSH)
- Patient Education as Topic
- Patient Participation
- Physician-Patient Relations
- Respiratory Tract Diseases - therapy
- Treatment Adherence and Compliance
- Specialty
- Health Education
- Pulmonary Medicine
- Abstract
- This book examines the most up-to-date strategies that can be used to enhance the healthcare professional-patient interaction to influence positive behavior change and improve treatment adherence in pulmonary healthcare. This book is written by experts in the field who couple their experience with practical strategies (the art) with evidence-based theory (the science). Chapters discuss global concepts such as motivational interviewing on improving engagement and how to apply strategies to specific situations (for examples: smoking cessation, promoting physical activity, inhaler adherence, supplemental oxygen use, and non-invasive ventilation) commonly experienced on the front lines of caring for patients with pulmonary disorders. The textbook raises awareness of direct approaches and recent technological advances that healthcare professionals can use to support positive behavior change in their day-to-day clinical practice. Effective, patient-tailored self-management interventions are discussed, including the evidence for these interventions and ways to personalize the strategies to each patient’s unique needs. This book is an ideal guide for healthcare professionals working with patients experiencing chronic pulmonary conditions, including pulmonologists, primary care physicians, physician assistants, nurses, trainees, and the many allied health professionals involved in delivering care such as respiratory therapists, pharmacists, and behavioral psychologists. The concepts of this book can also be applied to the management of other chronic diseases such as coronary artery disease and diabetes mellitus.
- Contents
- 1. Defining patient engagement, health behavior change, and disease self-management -- 2. Learning: developing knowledge through making meaning -- 3. Psychomotor skill development: learning what AND how to do -- 4. Best practice in educational design for patient learning -- 5. The impact of self-efficacy on behavior change: the roles of socio-cultural and mental health factors -- 6. Integrating motivational interviewing into pulmonary healthcare -- 7. Anxiety, depression, and using evidence-based techniques and strategies to support engagement and adherence -- 8. Technology to enhance engagement in physical activity -- 9. The role of mind-body approaches in promoting healthcare engagement and positive behavior change -- 10. Strategies to improve adherence to supplemental oxygen therapy -- 11. Self-management: personalized action plans for COPD exacerbations -- 12. Domiciliary noninvasive ventilation: strategies for improving adherence to home use -- 13. Teaching the practical skill of correct inhaler use: knowing and being able to do -- 14. Smoking cessation: breaking the strong addiction.
- Format
- e-Book
- Location
- Online
The Evolution and Everyday Practice of Collective Patient Involvement in Europe : An Examination of Policy Processes, Motivations, and Implementations in Four Countries
https://libcat.nshealth.ca/en/permalink/provcat42944
Alexander Haarmann.
--Cham:
Springer
, c2018.
- Available Online
- View e-Book
- Location
- Online
This timely study analyzes social, economic, political, provider, and patient factors shaping collective patient involvement in European health care from the postwar period to the present day. Examining representative countries England, the Netherlands, Germany, and Sweden, it documents the roles of providers and legislatures in facilitating consumer involvement, and the varied forms of patient input into hospital operations. These findings are compared and contrasted against the intent and ide…
- Available Online
- View e-Book
- Author
- Haarmann, Alexander
- Responsibility
- Alexander Haarmann
- Place of Publication
- Cham
- Publisher
- Springer
- Date of Publication
- c2018
- Physical Description
- 1 online resource (xxx, 350 p.
- ISBN
- 9783319645957
- 9783319645940 (print ed.)
- 9783319645964 (print ed.)
- 9783319878300 (print ed.)
- Subjects (MeSH)
- Delivery of Health Care
- Europe
- Inpatients
- Insurance, Health
- Organizational Case Studies
- Patient Participation
- Specialty
- Policy
- Sociology, Medical
- Abstract
- This timely study analyzes social, economic, political, provider, and patient factors shaping collective patient involvement in European health care from the postwar period to the present day. Examining representative countries England, the Netherlands, Germany, and Sweden, it documents the roles of providers and legislatures in facilitating consumer involvement, and the varied forms of patient input into hospital operations. These findings are compared and contrasted against the intent and ideals behind patient involvement to assess the effectiveness of implementation policy, strengths and drawbacks of patient participation, and patient satisfaction and outcomes. The book's conclusions identify emerging forms of patient participation andápredict the impact of health policy on the future of European collective patient involvement. Included in the coverage: Patient involvement: who, what for, and in what way? The Netherlands: the legislative process to collective patient involvement England: formal means of public involvement'a continuous story of discontinuity Germany: Joint Federal Committee'the "Little Legislator" Sweden: reasons for a late emergence of patient involvement Lessons to be learned from implementing patient involvement. The Evolution and Everyday Practice of Collective Patient Involvement in Europe will interest and inspire scholars and researchers in diverse fields, including social policy, sociology, political sciences, and nursing studies, as well as patient organizations, policymakers, and healthcare providers. .
- Contents
- Introduction -- Patient Involvement -- of Whom, What for, and in What Way? -- A Theoretical Framework for the Study -- Methodology and Study Design -- The Netherlands -- England -- Germany -- Sweden -- Comparison -- Bringing Four Cases Together -- Bibliography.
- Format
- e-Book
- Location
- Online
How engaged are Canadians in their primary care? : results from the 2010 Commonwealth Fund International Health Policy Survey
https://libcat.nshealth.ca/en/permalink/provcat25289
Health Council of Canada.
--Toronto, ON:
Health Council of Canada
, 2011.
- Call Number
- W 84.6 DC2 H847 2011
- Location
- Halifax Infirmary
- Call Number
- W 84.6 DC2 H847 2011
- Corporate Author
- Health Council of Canada
- Place of Publication
- Toronto, ON
- Publisher
- Health Council of Canada
- Date of Publication
- 2011
- Physical Description
- 31 p.
- Series Vol.
- bulletin 5
- Series Title
- Canadian health care matters
- ISBN
- 9781926961088
- Subjects (MeSH)
- Attitude to Health - Canada - Statistics
- Health Care Surveys - Canada
- Primary Health Care - statistics & numerical data - Canada
- Patient Participation - statistics & numerical data - Canada
- Format
- Book
- Location
- Halifax Infirmary
- Loan Period
- 3 weeks
Interpreting Health Benefits and Risks : A Practical Guide to Facilitate Doctor-Patient Communication
https://libcat.nshealth.ca/en/permalink/provcat33626
Erik Rifkin, Andrew Lazris.
--Cham:
Springer
, c2015.
- Available Online
- View e-Book
- Location
- Online
This timely guide to communication in patient-centered medicine argues for greater clarity in explaining health risks versus benefits of an array of screening tests, procedures, and drug regimens. It reviews the growing trend toward patients' involvement in their own care, particularly in terms of chronic conditions, and details approaches physicians can use to prepare patients (and themselves) for collaborative decision-making based on informed choices and meaningful knowledge. Chapters apply …
- Available Online
- View e-Book
- Author
- Rifkin, Erik
- Other Authors
- Lazris, Andrew
- Responsibility
- Erik Rifkin, Andrew Lazris
- Place of Publication
- Cham
- Publisher
- Springer
- Date of Publication
- c2015
- Physical Description
- 1 online resource (xx, 236 p.) : 50 illus.
- ISBN
- 9783319115443
- 9783319115436 (print ed.)
- Subjects (MeSH)
- Decision Making
- Diagnostic Techniques and Procedures - adverse effects
- Patient Participation
- Physician-Patient Relations
- Risk Assessment
- Therapeutics - adverse effects
- Abstract
- This timely guide to communication in patient-centered medicine argues for greater clarity in explaining health risks versus benefits of an array of screening tests, procedures, and drug regimens. It reviews the growing trend toward patients' involvement in their own care, particularly in terms of chronic conditions, and details approaches physicians can use to prepare patients (and themselves) for collaborative decision-making based on informed choices and meaningful knowledge. Chapters apply this lens to a wide range of common interventions as contentious as estrogen replacement therapy and antibiotics, and as widely prescribed as the daily aspirin and the annual physical. With this goal in mind, the authors also introduce an innovative decision-making tool that translates risks and benefits into a clear graphic format for fewer chances of miscommunication or misunderstanding. Among the topics covered: Involving the patient in decision making; BRCT: the Benefit/Risk Characterization Theater; Breast Cancer Screening--Mammograms; Prostate Cancer Screening; Statins, cholesterol, and coronary heart disease. Physicians in family and internal medicine will find Interpreting Health Benefits and Risks: A Practical Guide to Facilitate Doctor-Patient Communication a valuable resource for communicating with patients and new possibilities for working toward their better health and health education. This book considers several common and important situations where faulty decision-making makes overtreatment a serious risk. Clear, fair, referenced, and useful information is provided. And a powerful intuitive technique is introduced which allows patient and doctor to talk as equals as they work together in the exam room. As this book is accepted and its ideas and technique are extended, I feel sure that net harm to patients will be curtailed. And what is more, the integrity of the decision-making process will be improved. --Thomas Finucane, MD, Professor of Medicine, The Johns Hopkins University School of Medicine.
- Contents
- Part I. Setting the Stage -- Shared Decision Making -- Decision Aids -- Towards a Universal Decision Aid -- Involving the Patient in Decision Making -- BRCTs -- Part II. Case Studies : Health Benefits and Risks -- Breast Cancer Screening: Mammograms -- Colon Cancer Screening with Colonoscopy -- Prostate Cancer Screening -- Screening for Lung Cancer with Spiral CT -- Health Effects of Smoking -- Exercise Stress Tests -- The Use of Warfarin in Atrial Fibrillation -- Aspirin for Prevention of Heart Disease and Stroke -- Screening for Carotid Disease in Asymptomatic Patients -- Cholesterol Screening -- Statins, Cholesterol and Coronary Heart Disease -- Annual Exam -- Screening for and Treating Dementia -- Osteoporosis: Bone Density Testing and Drug Treatment -- Osteoporosis: Calcium and Vitamin D -- Estrogen Replacement Therapy -- Vitamins and Supplements -- MRI and Back Pain -- Antibiotics in Sinusitis and Bronchitis -- Final Thoughts.
- Format
- e-Book
- Publication Type
- Case Reports
- Location
- Online
A Journey Towards Patient-Centered Healthcare Quality : Patients, Families and Caregivers, Voices of Transformation
https://libcat.nshealth.ca/en/permalink/provcat45068
Jean Moody-Williams.
--Cham:
Springer
, c2020.
- Available Online
- View e-Book
- Location
- Online
This book provides valuable insight into emerging trends in healthcare delivery patient, family and caregiver engagement and the intersection of the two. It is unique in that it not only incorporates patient’s voice but provides context in the application of patients’ families and caregivers in healthcare transformation and the future of healthcare models. It is suited toward not only promoting empathy toward patients but also challenging the reader to learn and think about the future of health…
- Available Online
- View e-Book
- Author
- Moody-Williams, Jean
- Responsibility
- Jean Moody-Williams
- Place of Publication
- Cham
- Publisher
- Springer
- Date of Publication
- c2020
- Physical Description
- 1 online resource (xii, 113 p.) : 7 illus., 6 illus. in color
- ISBN
- 9783030263119
- 9783030263102 (Print ed.)
- 9783030263126 (Print ed.)
- Subjects (MeSH)
- Caregivers
- Delivery of Health Care
- Patient Participation
- Patient-Centered Care
- Professional-Family Relations
- Quality Improvement
- Specialty
- Health Services Administration
- Abstract
- This book provides valuable insight into emerging trends in healthcare delivery patient, family and caregiver engagement and the intersection of the two. It is unique in that it not only incorporates patient’s voice but provides context in the application of patients’ families and caregivers in healthcare transformation and the future of healthcare models. It is suited toward not only promoting empathy toward patients but also challenging the reader to learn and think about the future of healthcare and the value of patient’s voice in policy making and decisions about healthcare. It provides valuable information on quality improvement, consumer experience and emerging careers in this area with practical information and interventions. Nurses and other members of the care team play a critical role in the evolving models of care and must stay abreast of emerging trend to ensure that patients’ needs are met while contributing to meeting the quality and economic goals of the organizations and care settings in which they work. This book will help to ensure that they remain abreast of changing trends in quality improvement, quality measurement, cost, health information technology and patient and family engagement so that they are in a position to lead their teams and organizations. Direct accounts from patients, family and caregivers who want their “voices” heard are incorporated throughout the book.
- Contents
- 1. Understanding Patient and Family Engagement in Health Care -- 2. Consideration for Special Settings and Situations -- 3. Pursuing Continuous Quality Improvement -- 4. A Quest for Patient Safety -- 5. Consumer Information for Patients, Families, and Caregivers -- 6. Quality Measures for Patient, Family, and Caregiver Engagement -- 7. Considerations for Family and Caregivers and Crucial Conversations -- 8. Careers, Education, and Certifications in Patient and Family Engagement -- Appendix A: Roadmap for Patient and Family Engagement in Healthcare Practice and Research: Actions You Can Do Today -- Appendix B: To Err Is Human: Building a Safer Health System -- Appendix C: Crossing the Quality Chasm: A New Health System for the Twenty-First Century.
- Format
- e-Book
- Location
- Online
The knowledgeable patient : communication and participation in health
https://libcat.nshealth.ca/en/permalink/provcat27945
Hill, Sophie.
--Mississauga, ON:
Wiley
, 2011.
- Available Online
- View e-Book
- Location
- Online
- Available Online
- View e-Book
- Author
- Hill, Sophie
- Place of Publication
- Mississauga, ON
- Publisher
- Wiley
- Date of Publication
- 2011
- ISBN
- 9781444346855
- Subjects (MeSH)
- Evidence-Based Practice
- Health Communication
- Health Literacy
- Patient Education as Topic - methods
- Patient Participation
- Contents
- Does communication with consumers and carers need to improve? / Megan Prictor and Sophie Hill -- A new conceptual framework for advancing evidence-informed communication and participation / Sophie Hill and Mary Draper -- Interventions for communication and participation : their purpose and practice / Sophie Hill, Dianne Lowe and Rebecca E. Ryan -- Identifying outcomes of importance to consumers' communication and participation / Sophie Hill, Dianne Lowe and Joanne E. McKenzie -- Communicating risk and risk statistics for preventing chronic disease / Sophie Hill, Adrian G.K. Edwards and Dianne B. Lowe -- What does participation mean? reshaping our understanding of the meaning of surgery / Sophie Hill and Jessica Kaufman -- Disclosure : a case study of communication about medically-acquired risk for a rare disease / Rebecca E. Ryan, Jessica Kaufman and Sophie Hill -- How I used a systematic review from the Cochrane Library / Helen Dilkes, Jessica Kaufman and Sophie Hill -- Evidence and resources for system decision making : improving the experience of health and treatment / Dianne B. Lowe, Sophie Hill and Rebecca E. Ryan -- Looking at online health information more critically / John Kis-Rigo -- Learning to communicate / Megan Prictor ... [et al.] -- Getting the most out of research : using what we know / Dell Horey, Jessica Kaufman and Sophie Hill -- Research agendas for knowledgeable patients / Ruth Stewart and Sandy Oliver -- Managing multiple health problems : is there evidence to support consumer-focused communication and participation? / Rebecca E. Ryan and Sophie Hill -- Partners in care : an evidence-informed approach to improving communication with women in a hospital setting / Sophie Hill, Maureen Johnson and Mary Draper -- Building health literate societies / Sophie Hill ... [et al.] -- Tools for building research capacity and knowledge transfer / Helen Dilkes, Jessica Kaufman and Sophie Hill -- Emerging technologies for health communication / Yannis Pappas and Josip Car.
- Format
- e-Book
- Location
- Online
The Knowledgeable patient : communication and participation in health
https://libcat.nshealth.ca/en/permalink/provcat54549
Hill, Sophie.
--West Sussex, England:
Wiley-Blackwell
, 2011.
- Call Number
- W 85 K56 2011
- Location
- IWK Health Sciences Library
- Call Number
- W 85 K56 2011
- Author
- Hill, Sophie
- Place of Publication
- West Sussex, England
- Publisher
- Wiley-Blackwell
- Date of Publication
- 2011
- Physical Description
- 223 p.
- ISBN
- 9.78E+12
- Subjects (MeSH)
- Patient Education as Topic
- Health Communication
- Patient Participation
- Professional-Patient Relations
- Format
- Book
- Location
- IWK Health Sciences Library
- Copies
- 1
- Loan Period
- 2 weeks
Medical decision making : a physician's guide
https://libcat.nshealth.ca/en/permalink/provcat23516
Schwartz, Alan.
--Cambridge, England:
Cambridge University Press
, 2008.
- Call Number
- W 61 S411m 2008
- Location
- Dickson Building
- Call Number
- W 61 S411m 2008
- Author
- Schwartz, Alan
- Other Authors
- Bergus, George
- Place of Publication
- Cambridge, England
- Publisher
- Cambridge University Press
- Date of Publication
- 2008
- Physical Description
- 211 p.
- ISBN
- 9780521697699
- Subjects (MeSH)
- Clinical Decision-Making
- Ethics, Medical
- Informed Consent
- Patient Participation
- Physician-Patient Relations
- Treatment Outcome
- Format
- Book
- Location
- Dickson Building
- Copies
- 1
- Loan Period
- 3 weeks
Meeting the physical therapy needs of children
https://libcat.nshealth.ca/en/permalink/provcat53823
Effgen, Susan K.
--Philadelphia, PA:
F.A. Davis Co.
, 2005.
- Call Number
- WS 368 M495 2005
- Location
- IWK Health Sciences Library
- Call Number
- WS 368 M495 2005
- Author
- Effgen, Susan K.
- Place of Publication
- Philadelphia, PA
- Publisher
- F.A. Davis Co.
- Date of Publication
- 2005
- Physical Description
- 568 p. : ill.
- ISBN
- 803602502
- Subjects (MeSH)
- Physical Therapy Techniques
- Health Facility Environment
- Needs Assessment
- Patient Participation
- Child
- Infant
- Adolescent
- Format
- Book
- Location
- IWK Health Sciences Library
- Copies
- 1
- Loan Period
- 2 weeks
Occupational therapy in mental health : a vision for participation
https://libcat.nshealth.ca/en/permalink/provcat33509
editors, Catana Brown, Virginia C. Stoffel ; associate editor, Jaime Phillip Muñoz.
--Philadelphia, PA:
F.A. Davis Co
, c2011.
- Available Online
- View e-Book
- Holdings
- Cape Breton Regional: 2000 - 2006.
- Nova Scotia Hospital: v. 2, 1982 - v. 21, 2005.
- Location
- Online
This text distinguishes what occupational therapists offer to mental health practice across the life span. It features a client-centered, recovery oriented approach to empower patients to be in control of their own lives and to recognize the contribution of occupational therapy in promoting full participation in daily life. It explains the recovery process for all areas of patients' lives, physical, emotional, spiritual, and mental, and how to manage co-ocurring conditions. This text gives voi…
- Available Online
- View e-Book
- Other Authors
- Brown, Catana
- Stoffel, Virginia
- Munoz, Jaime Phillip
- Responsibility
- editors, Catana Brown, Virginia C. Stoffel ; associate editor, Jaime Phillip Muñoz
- Place of Publication
- Philadelphia, PA
- Publisher
- F.A. Davis Co
- Date of Publication
- c2011
- Holdings
- Cape Breton Regional: 2000 - 2006.
- Nova Scotia Hospital: v. 2, 1982 - v. 21, 2005.
- Physical Description
- 1 online resource (xxxii, 811 p.)
- ISBN
- 9780803625105 (electronic bk.)
- 9780803617049
- ISSN
- 0164-212X
- Subjects (LCSH)
- Occupational therapy
- Mentally ill - Rehabilitation
- Mental Disorders - therapy
- Occupational Therapy - methods
- Patient Participation
- Abstract
- This text distinguishes what occupational therapists offer to mental health practice across the life span. It features a client-centered, recovery oriented approach to empower patients to be in control of their own lives and to recognize the contribution of occupational therapy in promoting full participation in daily life. It explains the recovery process for all areas of patients' lives, physical, emotional, spiritual, and mental, and how to manage co-ocurring conditions. This text gives voice to the lived experience of mental illness across the life span. It serves as a guide through assessment and interventions for individuals with mental health conditions and those whose life circumstances generate significant challenges to their participation in valued activities. Key features include: Person-Environment-Occupation (PEO) Model: the organizing principle for this text frames an occupational performance, client-centered, and evidenced-based approach to occupational therapy in mental health; The "lived experience" of mental illness and recovery across the life span: individuals in recovery and their families share their perspectives through photographs and narratives, providing OTs with insights that enable them to better understand the lived experience; Assessment and intervention: more than 230 evidence-based and theoretically grounded assessments and interventions address psychosocial issues; Diagnoses: thorough definitions and discussions emphasize their impact on occupational performance; Environments: full chapters highlight the importance of context, describing the different settings in which occupational therapists work and the environmental factors that impact the lives of individuals in recovery; International expertise: renowned contributors from around the globe share their wealth of knowledge -- From book cover.
- Contents
- Part 1. Foundations -- Recovery -- History of mental health: perspectives of consumers and practitioners -- Person-Environment-Occupation Model -- Psychosocial concerns with disability -- Evidence-based practice in mental health -- Part 2. The Person -- Section 1. Introduction -- Introduction to the person -- Section 2. Diagnosis -- Pervasive developmental disorders -- Attention and disruptive behavior disorders -- Intellectual disabilities -- Eating disorders -- Personality disorders -- Mood disorders -- Anxiety disorders -- Schizophrenia -- Substance-related disorders -- Co-occurring disorders -- Dementia -- Section 3. Client Factors -- Cognitive skills -- Cognitive beliefs -- Sensory skills -- Communication and social skills -- Coping skills -- Motivation -- Emotion regulation -- Pain regulation -- Part 3. Environment -- Section 1. Introduction -- Introduction to the environment -- Section 2. Environments -- The political and public policy environment -- Attitudinal environment and stigma -- Families living with mental illness -- Mental health practice in a multicultural context -- The spiritual environment -- The neighborhood and community -- Supported housing: creating a sense of home -- Section 3. Practice settings -- Early intervention: a practice setting for infant and toddler mental health -- Consumer-operated services -- After-school programs -- Mental health practice in forensic settings -- State hospitals -- Psychosocial clubhouses -- Community-based case management -- Hospital-based mental health care -- Mental illness in the workplace: policies and practices that impact disability -- Homeless and women's shelters -- Wraparound services: children and families -- Part 4. Occupation -- Section 1. Introduction -- Introduction to occupation and co-occupation -- Section 2. Occupations -- Occupation and wellness -- Activities of daily living and instrumental activities of daily living -- Student: K through 12 -- Student: adult education -- Work as occupation --Social participation -- Leisure and play -- Rest and sleep -- Spiritual occupation -- Grief and bereavement -- Glossary -- Index of Assessments -- Index of Interventions.
- Format
- e-Book
- Location
- Online
Occupational therapy in mental health : a vision for participation
https://libcat.nshealth.ca/en/permalink/provcat24710
Brown, Catana.
--Philadelphia, PA:
F.A. Davis
, 2010.
- Call Number
- WM 450.5.02 B877o 2011
- Holdings
- Cape Breton Regional: 2000 - 2006.
- Nova Scotia Hospital: v. 2, 1982 - v. 21, 2005.
- Location
- Nova Scotia Hospital
- Call Number
- WM 450.5.02 B877o 2011
- Author
- Brown, Catana
- Other Authors
- Stoffel, Virginia C.
- Place of Publication
- Philadelphia, PA
- Publisher
- F.A. Davis
- Date of Publication
- 2010
- Holdings
- Cape Breton Regional: 2000 - 2006.
- Nova Scotia Hospital: v. 2, 1982 - v. 21, 2005.
- Physical Description
- 811 p.
- ISBN
- 9780803617049
- ISSN
- 0164-212X
- Subjects (MeSH)
- Occupational Therapy
- Mentally Disabled Persons - rehabilitation
- Mental Disorders - therapy
- Patient Participation
- Format
- Book
- Location
- Nova Scotia Hospital
- Loan Period
- 3 weeks
Patient-centered medicine : transforming the clinical methods
https://libcat.nshealth.ca/en/permalink/provcat22931
Stewart, Moira.
--Thousand Oaks, CA:
Sage Publications
, 1995.
- Call Number
- W 84 P298 1995
- Location
- Dickson Building
- Call Number
- W 84 P298 1995
- Author
- Stewart, Moira
- Place of Publication
- Thousand Oaks, CA
- Publisher
- Sage Publications
- Date of Publication
- 1995
- Physical Description
- 267 p.
- ISBN
- 0803956894
- Subjects (MeSH)
- Patient-Centered Care
- Physician-Patient Relations
- Patient Participation
- Patient Satisfaction
- Delivery of Health Care - methods
- Format
- Book
- Location
- Dickson Building
- Loan Period
- 3 weeks
Patient Involvement in Health Technology Assessment
https://libcat.nshealth.ca/en/permalink/provcat41987
Karen M. Facey, Helle Ploug Hansen, Ann N.V. Single, editors.
--Singapore:
Adis
, 2017.
- Available Online
- View e-Book
- Location
- Online
"If you're not involving patients, you're not doing HTA!" - Dr. Brian O'Rourke, President and CEO of CADTH, Chair of INAHTA. This is the first book to offer a comprehensive guide to involving patients in health technology assessment (HTA). Defining patient involvement as patient participation in the HTA process and research into patient aspects, this book includes detailed explanations of approaches to participation and research, as well as case studies. Patient Involvement in HTA enables resea…
- Available Online
- View e-Book
- Other Authors
- Facey, Karen M.
- Hansen, Helle Ploug
- Single, Ann N.V.
- Responsibility
- Karen M. Facey, Helle Ploug Hansen, Ann N.V. Single, editors
- Place of Publication
- Singapore
- Publisher
- Adis
- Date of Publication
- 2017
- Physical Description
- 1 online resource (xxvi, 434 pages) : 20 illus., 15 illus. in color
- ISBN
- 9789811040689
- 9789811040672 (print ed.)
- Subjects (MeSH)
- Comparative Effectiveness Research - ethics
- Organizational Case Studies
- Patient Participation
- Technology Assessment, Biomedical - ethics
- Technology Assessment, Biomedical - methods
- Abstract
- "If you're not involving patients, you're not doing HTA!" - Dr. Brian O'Rourke, President and CEO of CADTH, Chair of INAHTA. This is the first book to offer a comprehensive guide to involving patients in health technology assessment (HTA). Defining patient involvement as patient participation in the HTA process and research into patient aspects, this book includes detailed explanations of approaches to participation and research, as well as case studies. Patient Involvement in HTA enables researchers, postgraduate students, HTA professionals and experts in the HTA community to study these complementary ways of taking account of patients' knowledge, experiences, needs and preferences. Part I includes chapters discussing the ethical rationale, terminology, patient-based evidence, participation and patient input. Part II sets out methodology including: Qualitative Evidence Synthesis, Discrete Choice Experiments, Analytical Hierarchy Processes, Ethnographic Fieldwork, Deliberative Methods, Social Media Analysis, Patient-Reported Outcome Measures, patients as collaborative research partners and evaluation. Part III contains 15 case studies setting out current activities by HTA bodies on five continents, health technology developers and patient organisations. Each part includes discussion chapters from leading experts in patient involvement. A final chapter reflects on the need to clearly define the goals for patient involvement within the context of the HTA to identify the optimal approach. With cohesive contributions from more than 80 authors from a variety of disciplines around the globe, it is hoped this book will serve as a catalyst for collaboration to further develop patient involvement to improve HTA.
- Contents
- Part I: Conceptualisation -- 1. Health Technology Assessment -- 2. Exploring Ethical Rationales -- 3. Reflections on Terms, Goals and Organisation -- 4. Patient-Based Evidence in HTA -- 5. Developing the Mosaic of Patient Participation in HTA -- 6. Patient Input to HTA -- 7. Discussion: Attending to Values and Quality of Patient Involvement in HTA -- Part II: Methodologies -- 8. Patients as Collaborative Partners in Clinical Research to Inform HTA -- 9. Developing Patient-Reported and Relevant Outcome Measures -- 10. Discrete Choice Experiments -- 11. Analytic Hierarchy Process -- 12. Ethnographic Fieldwork -- 14. Deliberative Methods to Involve Patients in HTA -- 15. Qualitative Evidence Synthesis -- 16. Evaluation of Patient Involvement in HTA -- 17. Discussion: Making Sense of Patients' Perspectives, Experiences and Preferences in HTA -- 18. Discussion: Research to Promote Patient-Based HTA -- Part III: Country Approaches and Stakeholder Views -- 19. Australia -- 20. Brazil -- 21. Canada -- 22. Denmark -- 23. England -- 24. EUnetHTA: Patients’ Perspectives in the HTA Core Model® -- 25. Germany -- 26. Italy -- 27. Scotland -- 28. Sweden -- 29. Taiwan -- 30. USA: Comparative Effectiveness Research -- 31. Discussion of Approaches in Different Countries -- 32. Discussion: Patient Participation in HTA; Evidence of Real Change? -- 33. Patient Involvement in Medicine Development and Assessment -- 34. Medical Technologies: Involving Patients in Development and Assessment -- 35. Role of Patient Organisations -- 36. Discussion: Perspective of an HTA Appraisal Committee Chair -- 37. Reflections for Future Development.
- Format
- e-Book
- Location
- Online
Promoting aboriginal health : the family wellbeing empowerment approach
https://libcat.nshealth.ca/en/permalink/provcat40993
Mary Whiteside, Komla Tsey, Yvonne Cadet-James, Janya McCalman.
--Cham, Switzerland:
Springer
, c2014.
- Available Online
- View e-Book
- Location
- Online
"Family Wellbeing [Program] was developed in 1993 by the Aboriginal Education Development Branch (AEDB) of the South Australian Department of Education, Training and Employment. The program began as part of South Australia's state-wide response to the Royal Commission into Aboriginal Deaths in Custody" -- page 1.
- Available Online
- View e-Book
- Author
- Whiteside, Mary
- Other Authors
- Tsey, Komla
- Cadet-James, Yvonne
- McCalman, Janya, 1958-
- Responsibility
- Mary Whiteside, Komla Tsey, Yvonne Cadet-James, Janya McCalman
- Place of Publication
- Cham, Switzerland
- Publisher
- Springer
- Date of Publication
- c2014
- Physical Description
- 1 online resource (xvi, 54 pages : illustrations)
- ISBN
- 9783319046181
- 9783319046174 (print ed.)
- Subjects (MeSH)
- Family Health
- Health Promotion
- Oceanic Ancestry Group
- Patient Participation
- Public Health
- Other Subjects
- Australia
- Abstract
- "Family Wellbeing [Program] was developed in 1993 by the Aboriginal Education Development Branch (AEDB) of the South Australian Department of Education, Training and Employment. The program began as part of South Australia's state-wide response to the Royal Commission into Aboriginal Deaths in Custody" -- page 1.
- Contents
- 1. The Family Wellbeing Empowerment Program -- Program Development -- Current Family Wellbeing Delivery -- 2. The Research Approach -- The Empowerment Research Program -- Methodology for a Theoretical Study -- 3. An Aboriginal Family Wellbeing Model of Empowerment -- The Social Environment -- Joy's Story -- 4. Beliefs and Attitudes -- Choice -- Responsibility -- A Positive Attitude -- Self-Esteem and Pride -- Spirituality -- Personal Values -- Alison's Story -- 5. Skills and Knowledge -- Life Experience -- Emotional Control -- Analytic Skills -- Communication Skills -- Skills for Helping Others -- Ron's Story -- 6. Agency -- Healing -- Planning for the Future -- Improving Relationships -- Helping Others -- Community Efforts for Change -- Nancy's Story -- 7. Outcomes -- Personal Healing and Growth -- Better Relationships -- Confident and Engaged at Work -- Community Responsibilities -- Helping Others to Change -- Community Change -- Tom's Story -- 8. Conclusion.
- Format
- e-Book
- Location
- Online
Self-management of depression : a manual for mental health and primary care professionals
https://libcat.nshealth.ca/en/permalink/provcat24876
Yeung, Albert.
--Cambridge, England:
Cambridge University Press
, 2010.
- Call Number
- WM 171 Y48s 2010
- Location
- Nova Scotia Hospital
- Call Number
- WM 171 Y48s 2010
- Author
- Yeung, Albert
- Other Authors
- Feldman, Greg
- Fava, Maurizio
- Place of Publication
- Cambridge, England
- Publisher
- Cambridge University Press
- Date of Publication
- 2010
- Physical Description
- 206 p.
- ISBN
- 9780521710084
- Subjects (MeSH)
- Patient Participation
- Psychotherapy - methods
- Self Care - methods
- Format
- Book
- Location
- Nova Scotia Hospital
- Loan Period
- 3 weeks
